A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223477



Internal ID20790517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63312501..63395000hg38UCSC Ensembl
chr9:67267473..67349972hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3882500
hg1982500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441063
Supporting Variants
Samples
Known GenesAQP7P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223477
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00216


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer